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80605

(+)-α-Pinene

analytical standard

Synonym(s):

(1R,5R)-2,6,6-Trimethylbicyclo[3.1.1]hept-2-ene, (1R,5R)-2-Pinene

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About This Item

Empirical Formula (Hill Notation):
C10H16
CAS Number:
7785-70-8
Molecular Weight:
136.23
UNSPSC Code:
85151701
NACRES:
NA.24
PubChem Substance ID:
329768986
EC Number:
232-087-8
Beilstein/REAXYS Number:
2038653
MDL number:
MFCD00001346
Technical Service
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grade

analytical standard

Quality Level

100

assay

≥98.5% ((sum of enantiomers), GC)

optical activity

[α]20/D +51±2°, neat

optical purity

enantiomeric ratio: ≥90:10% (GC)

autoignition temp.

491 °F

shelf life

limited shelf life, expiry date on the label

technique(s)

HPLC: suitable, gas chromatography (GC): suitable

refractive index

n20/D 1.465 (lit.)

bp

155-156 °C (lit.)

mp

−62 °C (lit.)

density

0.858 g/mL at 20 °C (lit.)

application(s)

cleaning products
cosmetics
flavors and fragrances
food and beverages
personal care

format

neat

storage temp.

2-8°C

SMILES string

CC1=CC[C@@H]2C[C@H]1C2(C)C

InChI

1S/C10H16/c1-7-4-5-8-6-9(7)10(8,2)3/h4,8-9H,5-6H2,1-3H3/t8-,9-/m1/s1

InChI key

GRWFGVWFFZKLTI-RKDXNWHRSA-N

General description

(+)-α-Pinene is a monoterpenoid compound, which comprises of an endocyclic double bond and is found in the resins of pine trees and other conifers.

Application

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

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Danger

Hazard Classifications

Aquatic Acute 1 - Aquatic Chronic 1 - Asp. Tox. 1 - Flam. Liq. 3 - Skin Irrit. 2 - Skin Sens. 1

Storage Class

3 - Flammable liquids

wgk

WGK 3

flash_point_f

91.4 °F - closed cup

flash_point_c

33 °C - closed cup

ppe

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter

Regulatory Information

危险化学品

This item has

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Certificates of Analysis (COA)

Lot/Batch Number
BCCN9868
BCCM7340
BCCJ1134
BCCG6386
BCCB9892

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Justin J Miller et al.
ACS infectious diseases, 6(10), 2567-2572 (2020-09-24)
Infection with malarial parasites renders hosts more mosquito-attractive than their uninfected, healthy counterparts. One volatile organic compound, α-pinene, is associated with Plasmodium spp. infection in multiple studies and is a known mosquito attractant. However, how malarial infection results in elevated
Seinfeld.HJ and Pandis.NS et al.
Atmospheric Chemistry and Physics: From Air Pollution to Climate Change, (3) (2016)

Global Trade Item Number

SKUGTIN
592439-5G04061833356579
80605-1ML04061832980416
80605-5ML04061832980904